Considerations for Familial Chylomicronemia Diagnosis in the Era of Next-Generation Sequencing: A Latin American Perspective-Reference-Cited by-同舟云学术

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Considerations for Familial Chylomicronemia Diagnosis in the Era of Next-Generation Sequencing: A Latin American Perspective

Published:2024 Issue: Volume:12 Page:
ISSN:2326-4594
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:
Short-container-title:J. inborn errors metab. screen.

Author:

Lourenco Charles Marques¹^ORCID,Corral Pablo²,Santos Raul D.³^ORCID,Nogueira Juan Patricio⁴,Mendivil Carlos O.⁵^ORCID,Santos José L.⁶,Pachajoa Harry⁷,Bañares Virginia⁸,Mattos-Velez Maria Belen⁹

Affiliation:

1. Faculdade de Medicina de São José do Rio Preto, Brazil

2. FASTA University, Argentina

3. Universidade de São Paulo, Brazil

4. Universidad Nacional de Formosa, Argentina

5. Universidad de los Andes, Colombia

6. Pontificia Universidad Católica de Chile, Chile

7. Universidad Icesi, Colombia

8. Centro Nacional de Genética Médica, Argentina

9. Hospital de Especialidades Carlos Andrade Marín, Ecuador

Publisher

FapUNIFESP (SciELO)

Link

http://www.scielo.br/scielo.php?script=sci_pdf&pid=S2326-45942024000100401&tlng=en

Reference25 articles.

1. Diagnostic algorithm for familial chylomicronemia syndrome;Stroes E;Atheroscler Suppl,2017

2. Familial chylomicronemia syndrome: An under-recognized cause of severe hypertriglyceridaemia;Baass A;J Intern Med,2020

3. Familial chylomicronemia syndrome: A clinical guide for endocrinologists;Falko JM;Endocr Pract,2018

4. The chylomicronemia syndrome is most often multifactorial: A narrative review of causes and treatment;Chait A;Ann Intern Med,2019

5. Severe hypertriglyceridemia presenting as eruptive xanthomatosis;Vangara SS;J Family Med Prim Care,2018

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